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Effects of thoracic approach to thoracic paravertebral blockade performed via video - assisted thoracoscopy on postoperative analgesia in patients undergoing Single-port thoracoscopic lobectomy

Effects of thoracic approach to thoracic paravertebral blockade performed via video - assisted thoracoscopy on postoperative analgesia in patients undergoing Single-port thoracoscopic lobectomy

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100049416
Enrollment
Unknown
Registered
2021-08-02
Start date
2021-08-16
Completion date
Unknown
Last updated
2022-04-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Lung Cancer

Interventions

Experimental group:Paravertebral nerve block group through thoracic approach under thoracoscopy
Control group:Ultrasound guided percutaneous paraspinal nerve block

Sponsors

Army Medical Center of PLA
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Preoperative imaging and (or) pathology are considered to be lung cancer, and single-port thoracoscopic lobectomy or segmentectomy is planned; 2. Although preoperative imaging and (or) pathology are considered benign lesions, single-port thoracoscopic lobectomy or segmentectomy is planned; 3. Aged 18 to 75 years.

Exclusion criteria

Exclusion criteria: 1. Forced expiratory volume in one second (forced expiratory volume in one second, FEVl%)<=60%; 2. Combined with coagulation dysfunction, skin infection at the puncture site, local anesthetic allergy and other nerve block contraindications; 3. Patients with severe cardiovascular and cerebrovascular diseases, liver and kidney insufficiency; 4. History of previous ipsilateral chest surgery; 5. Long-term chronic pain, psychological or psychiatric history, and long-term application history of antipyretic and analgesic drugs; 6. Thoracic or spinal deformity; 7. Unable to understand and cooperate with nerve block operation or postoperative visual analog score; 8. Long-term alcoholism patients; 9. Participate in other trials within three months.

Design outcomes

Primary

MeasureTime frame
Dosage of anesthetic drugs;Visual analogous scale;Pulmonary function rehabilitation;Anxiety and depression assessment;Complications of paravertebral nerve block;

Secondary

MeasureTime frame
Paravertebral nerve block operation time;Times of rescue analgesia;

Countries

China

Contacts

Public ContactJiang Bin

Army Medical Center of PLA

1275301534@qq.com+86 17723041984

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026